Product Recalls in New Hampshire

Product recalls affecting New Hampshire — including food, drugs, consumer products, medical devices, and vehicles distributed to New Hampshire. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,540 recalls have been distributed to New Hampshire in the last 12 months.

49,311 total recalls
2,540 in last 12 months

Showing 73817400 of 49,311 recalls

FoodOctober 19, 2023· Nature'S Path Foods Inc

Recalled Item: Nature's Path Organic Pumpkin Spice Waffles Recalled by Nature'S Path Foods...

The Issue: undeclared peanut

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodOctober 19, 2023· Nature'S Path Foods Inc

Recalled Item: Nature's Path Organic Dark Chocolate Chip Waffles Recalled by Nature'S Path...

The Issue: undeclared peanut

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 19, 2023· Siemens Healthcare Diagnostics Inc

Recalled Item: epoc NXS Host Blood Analysis System Recalled by Siemens Healthcare...

The Issue: Siemens Healthcare Diagnostics Inc. has confirmed a potential issue that...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2023· Meridian Bioscience Inc

Recalled Item: Cardinal Health Clean Stool Transportation System-For the collection...

The Issue: Due to a manufacturing defect, certain Para-Pak vials may be at risk for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2023· Meridian Bioscience Inc

Recalled Item: Para-Pak Zn-PVA/10% Formalin-for the routine collection Recalled by Meridian...

The Issue: Plastic vials contain a manufacturing defect may cause an increased risk of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2023· Meridian Bioscience Inc

Recalled Item: Para-Pak Clean Vial-For the collection Recalled by Meridian Bioscience Inc...

The Issue: Plastic vials contain a manufacturing defect may cause an increased risk of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2023· Integra LifeSciences Corp.

Recalled Item: Integra Cranial Access Kit - For access to the subarachnoid Recalled by...

The Issue: Defect in the outer packaging of the Cranial Access Kits. can cause the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2023· Integra LifeSciences Corp.

Recalled Item: Integra Cranial access kit (without Prep solutions) Bit and Guard-For...

The Issue: Defect in the outer packaging of the Cranial Access Kits can cause the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2023· Integra LifeSciences Corp.

Recalled Item: Integra Cranial Access Kit-For access to the subarachnoid space or Recalled...

The Issue: Defect in the outer packaging of the Cranial Access Kits. can cause the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2023· Integra LifeSciences Corp.

Recalled Item: Integra¿ Cranial Access Kit-For access to the subarachnoid space or Recalled...

The Issue: Defect in the outer packaging of the Cranial Access Kits. can cause the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2023· Integra LifeSciences Corp.

Recalled Item: Integra Cranial Access Kit -For access to the subarachnoid space Recalled by...

The Issue: Defect in the outer packaging of the Cranial Access Kits can cause the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2023· Integra LifeSciences Corp.

Recalled Item: Integra Cranial Access Kit-For access to the subarachnoid space or Recalled...

The Issue: Defect in the outer packaging of the Cranial Access Kits. can cause the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2023· Integra LifeSciences Corp.

Recalled Item: Integra Cranial Access Kit- For access to the subarachnoid space Recalled by...

The Issue: Defect in the outer packaging of the Cranial Access Kits. can cause the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2023· Integra LifeSciences Corp.

Recalled Item: Integra¿ Cranial Access Kit-For access to the subarachnoid space or Recalled...

The Issue: Defect in the outer packaging of the Cranial Access Kits. can cause the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2023· Integra LifeSciences Corp.

Recalled Item: Combo Kit Consists OF 10-110/INS-4500/INS-7040- For access to the...

The Issue: Defect in the outer packaging of the Cranial Access Kits. can cause the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugOctober 18, 2023· Exela Pharma Sciences LLC

Recalled Item: ELCYS (cysteine hydrochloride injection) Recalled by Exela Pharma Sciences...

The Issue: Presence of Particulate Matter: Silicone

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugOctober 18, 2023· Exela Pharma Sciences LLC

Recalled Item: 8.4% Sodium Bicarbonate Injection Recalled by Exela Pharma Sciences LLC Due...

The Issue: Presence of Particulate Matter: Silicone

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugOctober 18, 2023· Exela Pharma Sciences LLC

Recalled Item: Midazolam in 0.8% Sodium Chloride Injection 100 mg/100 mL (1mg/mL) Recalled...

The Issue: Presence of Particulate Matter: Silicone

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugOctober 18, 2023· VistaPharm LLC

Recalled Item: Sucralfate Oral Suspension Recalled by VistaPharm LLC Due to Microbial...

The Issue: Microbial Contamination of Non-Sterile Products: identified as Bacillus cereus.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 18, 2023· AURIS HEALTH INC

Recalled Item: Monarch Platform 100-240V- 50/60Hz 1440w Recalled by AURIS HEALTH INC Due to...

The Issue: Their is the potential that software issues may result in flipped image of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing